Device recall
Z-2050-2015: PowerPICC SOLO2 Catheter 4F Maximal Barrier Tray with Microintroducer…
FDA device recall · Class III · Bard Access Systems
Key facts
| Recall number (Z-number) | Z-2050-2015 |
|---|---|
| Recall event | 71420 |
| Product | PowerPICC SOLO2 Catheter 4F Maximal Barrier Tray with Microintroducer (Single-Lumen) (Sherlock) The PowerPICC Solo catheters are intended for short or long term peripheral access to the central venous system for intravenous therapy and blood sampling. |
| Product code | LJS |
| Recalling firm | Bard Access Systems |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Feb 10, 2016 |
| 510(k) numbers | K072230, K091324 |
| FEI number | 3006260740 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database